Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renata Catalano"'
Autor:
Daniela Cilloni, Francesca Messa, Francesca Arruga, Ilaria Defilippi, Enrico Gottardi, Milena Fava, Sonia Carturan, Renata Catalano, Enrico Bracco, Emanuela Messa, Paolo Nicoli, Daniela Diverio, Miguel A. Sanz, Giovanni Martinelli, Francesco Lo-Coco, Giuseppe Saglio
Publikováno v:
Haematologica, Vol 93, Iss 6 (2008)
The Wilms’ tumor gene WT1 is a reliable marker for minimal residual disease assessment in acute leukemia patients. The study was designed to demonstrate the potential use of WT1 to establish quality of remission in acute leukemia patients for early
Externí odkaz:
https://doaj.org/article/34c73617a1824b768290173a34b6de06
Autor:
Daniela Cilloni, Giuseppe Saglio, Annalisa Chiarenza, Francesca Messa, Marisa Pautasso, Enrico Bracco, Renata Catalano, Enrico Gottardi, Angelo Guerrasio, Ilaria Defilippi, Alessandro Morotti, Francesca Arruga, Riccardo Taulli, Sonia Carturan, Valentina Rosso, Daniela Baraban, Chiara Pilatrino
Publikováno v:
Cancer. 106:1188-1196
BACKGROUND The objective of this study was to evaluate the ability of the clinically available histone deacetylase (HDAC) inhibitor valproate to enhance the cytotoxicity of the Bcr-Abl inhibitor imatinib in imatinib-resistant cell lines. METHODS Inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04ff008227b8260d07c619adaa850913
https://doi.org/10.1002/cncr.21725
https://doi.org/10.1002/cncr.21725
Autor:
Emanuela Messa, Daniela Diverio, Enrico Gottardi, Miguel A. Sanz, Paolo Nicoli, Milena Fava, Daniela Cilloni, Francesca Messa, Sonia Carturan, Enrico Bracco, Giovanni Martinelli, Giuseppe Saglio, Francesca Arruga, Ilaria Defilippi, Renata Catalano, Francesco Lo-Coco
Publikováno v:
Haematologica. 93(6)
The Wilms' tumor gene WT1 is a reliable marker for minimal residual disease assessment in acute leukemia patients. The study was designed to demonstrate the potential use of WT1 to establish quality of remission in acute leukemia patients for early i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b27ab0e6cee89576b6aee90080d7c988
https://pubmed.ncbi.nlm.nih.gov/18443273
https://pubmed.ncbi.nlm.nih.gov/18443273
Autor:
Ilaria Iacobucci, Ilaria Defilippi, Alessandro Morotti, Paolo Nicoli, Francesca Messa, Enrico Bracco, Francesca Arruga, Giuseppe Saglio, Sonia Carturan, Valentina Rosso, Daniela Cilloni, Renata Catalano, Cristina Panuzzo, Emanuela Messa, Marisa Pautasso, Giovanni Martinelli
Publikováno v:
Leukemia. 22(6)
Mutations in nucleophosmin (NPM) exon 12 and the resulting delocalization of NPM into the cytoplasm are the most specific and frequent cellular events in acute myeloid leukemia patients (AML) with normal karyotype. Cytoplasmatic NPM (NPMc+) is associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbf83ba966a99c8dca6c445908c87ff1
https://pubmed.ncbi.nlm.nih.gov/20376085
https://pubmed.ncbi.nlm.nih.gov/20376085
Autor:
Francesca Messa, Renata Catalano, Marco Bosa, Alessandro Morotti, Enrico Bracco, Marisa Pautasso, Ilaria Defilippi, Guido Parvis, Daniela Cilloni, G. Saglio, Francesca Arruga, Valentina Rosso, Ubaldo Familiari, Sonia Carturan, Angelo Guerrasio
Publikováno v:
Leukemia. 21(6)
CD7/CD56-positive acute myeloid leukemias are characterized by constitutive phosphorylation of the NF-kB subunit p65 at Ser536
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc6db1ccb16197239a9c1e918cdac1e8
https://pubmed.ncbi.nlm.nih.gov/17377595
https://pubmed.ncbi.nlm.nih.gov/17377595
Autor:
Renata Catalano, Daniela Cilloni, Emanuela Messa, Sonia Carturan, Giuseppe Saglio, Valentina Rosso, Paolo Nicoli, Enrico Bracco, Francesca Messa, Francesca Arruga, Ilaria Defilippi
Publikováno v:
Annals of the New York Academy of Sciences. 1089
Recent advances in molecular genetics have increased knowledge regarding the mechanisms leading to myelodysplastic syndrome (MDS), secondary acute myeloid leukemia (AML), and therapy-induced MDS. Many genetic defects underlying MDS and AML have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1750f736c14365f903af4f54a1dff42c
https://pubmed.ncbi.nlm.nih.gov/17261784
https://pubmed.ncbi.nlm.nih.gov/17261784
Autor:
Emilia Giugliano, Ilaria Defilippi, Milena Fava, Paolo Nicoli, Michela Rondoni, Emanuela Messa, Giovanni Martinelli, Daniela Cilloni, Sonia Carturan, Emanuela Ottaviani, Simona Soverini, Giuseppe Saglio, Francesca Messa, Michele Baccarani, Valentina Rosso, Mario Tiribelli, Renata Catalano, Serena Merante, Francesca Arruga, Enrico Gottardi, Fabrizio Pane
Idiopathic hypereosinophilic syndromes (HES) comprise a spectrum of indolent to aggressive diseases characterized by persistent hypereosinophilia. Hypereosinophilia can result from the presence of a defect in the hematopoietic stem cell giving rise t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85175bde6b2f238d2462f992b7c6384e
http://hdl.handle.net/11588/108685
http://hdl.handle.net/11588/108685
Autor:
Renata Catalano, Giovanna Rege-Cambrin, Sonia Carturan, Francesca Arruga, Francesca Messa, Marisa Pautasso, Enrico Gottardi, Daniela Cilloni, Valentina Rosso, Alessandro Morotti, Enrico Bracco, Ilaria Defilippi, Giuseppe Saglio, Annalisa Chiarenza, Riccardo Taulli
NF-kB is a transcription factor that mediates antiapoptotic signals in several cancer cell lines. Here we have demonstrated that the cytotoxic drug, Etoposide, activates NF-kB in K562, a chronic myeloid leukemia blast crisis cell line. Treatment with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::003c58dfab9f4b028711f103bb23343a
http://hdl.handle.net/2318/148893
http://hdl.handle.net/2318/148893
Autor:
Enrico Gottardi, Renata Catalano, Riccardo Taulli, Valentina Rosso, Sonia Carturan, Marisa Pautasso, Giuseppe Saglio, Daniela Cilloni, Ilaria Defilippi, Annalisa Chiarenza, Francesca Arruga, Carola Ponzetto, Francesca Messa, Alessandro Morotti, Sara Capella
Introduction. Chronic Myeloid Leukemia (CML) is a myeloproliferative disorder caused by the Philadelphia translocation. Rare patients with a clinical presentation of CML are negative for the Ph chromosome. The pathogenesis of Ph negative CML is still
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1881099243bdd6834225a0ff7af989c
http://hdl.handle.net/2318/148942
http://hdl.handle.net/2318/148942
Autor:
Enrico Bracco, Renata Catalano, Valentina Rosso, Francesca Arruga, Sonia Carturan, Ilaria Defilippi, Emanuela Messa, C. Bittoto, Giuseppe Saglio, Francesca Messa, Daniela Cilloni, C. Boveri, Paolo Nicoli
Publikováno v:
Leukemia Research. 31:S60-S61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b23b6dcf13d5673fc14b0d8e008b4d20
https://doi.org/10.1016/s0145-2126(07)70106-6
https://doi.org/10.1016/s0145-2126(07)70106-6